Standout Papers

Mitochondrial DNA mutations in human disease 2005 2026 2012 2019 1.4k
  1. Mitochondrial DNA mutations in human disease (2005)
    Robert W. Taylor, Douglass M. Turnbull Nature Reviews Genetics
  2. High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease (2006)
    Andreas Bender, Kim J. Krishnan et al. Nature Genetics
  3. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease (2015)
    Gráinne S. Gorman, Andrew M. Schaefer et al. Annals of Neurology

Immediate Impact

14 by Nobel laureates 20 from Science/Nature 88 standout
Sub-graph 1 of 18

Citing Papers

Mitochondria at the crossroads of health and disease
2024 Standout
Ferroptosis regulation by the NGLY1/NFE2L1 pathway
2022 StandoutNobel
38 intermediate papers

Works of Robert W. Taylor being referenced

Mosaic dysfunction of mitophagy in mitochondrial muscle disease
2022
The genetics and pathology of mitochondrial disease
2016
and 48 more

Author Peers

Author Last Decade Papers Cites
Robert W. Taylor 17940 8816 2388 442 22.4k
Michio Hirano 15966 7597 2027 331 19.9k
Jan Smeıtınk 15425 6914 1281 346 21.8k
Massimo Zeviani 27619 12794 3191 410 32.8k
Patrick F. Chinnery 22514 9984 3812 478 28.4k
Eric A. Schon 19393 8776 2740 218 23.1k
Salvatore DiMauro 22466 12316 2781 399 28.9k
Nils‐Göran Larsson 19474 6384 2147 190 23.7k
Douglass M. Turnbull 28452 14346 4206 557 36.7k
David R. Thorburn 12936 6887 1045 230 15.8k
William L. Nyhan 8720 4594 824 443 14.3k

All Works

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Rankless by CCL
2026